A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987597



Internal ID59170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113520890..113521051hg38UCSC Ensembl
chr6:113842092..113842253hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458158
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987597
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002654


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